Medical Device Manufacturer · US , Scarborough , ME

Alere Scarborough, Inc. - FDA 510(k) Cleared Devices

17 submissions · 16 cleared · Since 2012
17
Total
16
Cleared
1
Denied

Alere Scarborough, Inc. has 16 FDA 510(k) cleared microbiology devices. Based in Scarborough, US.

Historical record: 16 cleared submissions from 2012 to 2019.

Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Alere Scarborough, Inc.

17 devices
1-12 of 17
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